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	1	Upregulation of adenosine A2A receptor in astrocytes is sufficient to trigger hippocampal multicellular dysfunctions and memory deficits Enthalten in Molecular psychiatry 23.7.2025: 1-15
	2	Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation Enthalten in Molecular psychiatry 14.8.2018: 1-17
	3	Association of modifiers and other genetic factors explain Marfan syndrome clinical variability Enthalten in European journal of human genetics 7.8.2018: 1-14
	4	A Difficult and Rare Diagnosis of Autoimmune Enteropathy in a Patient Affected by Down Syndrome Enthalten in Journal of clinical immunology 12.4.2016: 1-6
	5	Molecular Evidence of Reproductive Isolation in Sympatric Sibling Species of Mouse Lemurs Enthalten in International journal of primatology Bd. 23, Nr. 6, date:12.2002: 1335-1343
	6	Ameboma: an unusual cause of gastrointestinal bleeding during severe leptospirosis Enthalten in BMC infectious diseases Bd. 14, 2.6.2014, Nr. 1, date:12.2014: 1-6
	7	CA9 gene expression in conventional renal cell carcinoma: a potential marker for prediction of early metastasis after nephrectomy Enthalten in Clinical & experimental metastasis Bd. 24, 28.3.2007, Nr. 3, date:5.2007: 149-155
	8	Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease Enthalten in Nature genetics Bd. 54, 21.11.2022, Nr. 12, date:12.2022: 1786-1794
	9	Human genetic structure in Northwest France provides new insights into West European historical demography Enthalten in Nature Communications Bd. 15, 7.8.2024, Nr. 1, date:12.2024: 1-18
	10	Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing Enthalten in Translational Psychiatry Bd. 8, 5.12.2018, Nr. 1, date:12.2018: 1-7

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